Cargando…
Association of human platelet alloantigens encoding gene polymorphisms with the risk of Coronary artery disease in Iranian patients
BACKGROUND: Coronary artery disease (CAD) is characterized by narrowing/ blockade of coronary arteries that is mainly caused by atherosclerotic plaques. Considering the involvement of platelet abnormalities, such as defective aggregation and adhesion, in the cardiovascular-related disorders, genetic...
Autores principales: | Malakootikhah, Farideh, Naghavi, Hossein, Firouzabadi, Negar, Maadani, Mohsen, Shafiei, Massoumeh, Tajik, Nader |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856748/ https://www.ncbi.nlm.nih.gov/pubmed/33530946 http://dx.doi.org/10.1186/s12872-021-01892-z |
Ejemplares similares
-
Human platelet antigen 1-6, 9 and 15 in the Iranian population: An anthropological genetic analysis
por: Kazemi, Mohammad Hossein, et al.
Publicado: (2020) -
Hydroxylation index of omeprazole in relation to CYP2C19 polymorphism and sex in a healthy Iranian population
por: Payan, Maryam, et al.
Publicado: (2014) -
Platelets and platelet alloantigens: Lessons from human patients and animal models of fetal and neonatal alloimmune thrombocytopenia
por: Vadasz, Brian, et al.
Publicado: (2015) -
T cell tolerance to non-H-2-encoded stimulatory alloantigens is induced intrathymically but not prethymically
Publicado: (1983) -
Identification of two cis-encoded HLA-DQ molecules that carry distinct alloantigenic specificities
Publicado: (1984)